Devices and Methods for Delivering Energy as a Function of Condition Severity

ABSTRACT

A device for regulating energy delivery to an implanted circuit is disclosed. The device may include at least one implantable circuit and at least one pair of implantable electrodes in electrical communication with the circuit. The at least one pair of implantable electrodes may be configured to modulate at least one nerve. The at least one implantable circuit may be configured deliver a signal to the at least one pair of implantable electrodes. The signal may have at least one of a power level or a duration determined based on a severity of a detected physiologic condition.

RELATED APPLICATIONS

This application claims the benefit of priority under 35 U.S.C. §119(e)to U.S. Provisional Application No. 61/541,651, filed Sep. 30, 2011, andalso to U.S. Provisional Application No. 61/657,424, filed Jun. 8, 2012,all of which are incorporated herein by reference in their entirety.

TECHNICAL FIELD

Embodiments of the present disclosure generally relate to devices andmethods for modulating a nerve. More particularly, embodiments of thepresent disclosure relate to devices and methods for modulating a nervethrough the delivery of energy via an implantable electrical modulator.

BACKGROUND

Neural modulation presents the opportunity to treat many physiologicalconditions and disorders by interacting with the body's own naturalneural processes. Neural modulation includes inhibition (e.g. blockage),stimulation, modification, regulation, or therapeutic alteration ofactivity, electrical or chemical, in the central, peripheral, orautonomic nervous system. By modulating the activity of the nervoussystem, for example through the stimulation of nerves or the blockage ofnerve signals, several different goals may be achieved. Motor neuronsmay be stimulated at appropriate times to cause muscle contractions.Sensory neurons may be blocked, for instance to relieve pain, orstimulated, for instance to provide a signal to a subject. In otherexamples, modulation of the autonomic nervous system may be used toadjust various involuntary physiological parameters, such as heart rateand blood pressure. Neural modulation may provide the opportunity totreat several diseases or physiological conditions, a few examples ofwhich are described in detail below.

Among the conditions to which neural modulation may be applied isobstructive sleep apnea (OSA). OSA is a respiratory disordercharacterized by recurrent episodes of partial or complete obstructionof the upper airway during sleep. During the sleep of a person withoutOSA, the pharyngeal muscles relax during sleep and gradually collapse,narrowing the airway. The airway narrowing limits the effectiveness ofthe sleeper's breathing, causing a rise in CO₂ levels in the blood. Theincrease in CO₂ results in the pharyngeal muscles contracting to openthe airway to restore proper breathing. The largest of the pharyngealmuscles responsible for upper airway dilation is the genioglossusmuscle, which is one of several different muscles in the tongue. Thegenioglossus muscle is responsible for forward tongue movement and thestiffening of the anterior pharyngeal wall. In patients with OSA, theneuromuscular activity of the genioglossus muscle is decreased comparedto normal individuals, accounting for insufficient response andcontraction to open the airway as compared to a normal individual. Thislack of response contributes to a partial or total airway obstruction,which significantly limits the effectiveness of the sleeper's breathing.In OSA patients, there are often several airway obstruction eventsduring the night. Because of the obstruction, there is a gradualdecrease of oxygen levels in the blood (hypoxemia). Hypoxemia leads tonight time arousals, which may be registered by EEG, showing that thebrain awakes from any stage of sleep to a short arousal. During thearousal, there is a conscious breath or gasp, which resolves the airwayobstruction. An increase in sympathetic tone activity rate through therelease of hormones such as epinephrine and noradrenaline also oftenoccurs as a response to hypoxemia. As a result of the increase insympathetic tone, the heart enlarges in an attempt to pump more bloodand increase the blood pressure and heart rate, further arousing thepatient. After the resolution of the apnea event, as the patient returnsto sleep, the airway collapses again, leading to further arousals.

These repeated arousals, combined with repeated hypoxemia, leaves thepatient sleep deprived, which leads to daytime somnolence and worsenscognitive function. This cycle can repeat itself up to hundreds of timesper night in severe patients. Thus, the repeated fluctuations in andsympathetic tone and episodes of elevated blood pressure during thenight evolve to high blood pressure through the entire day.Subsequently, high blood pressure and increased heart rate may causeother diseases.

Efforts for treating OSA include Continuous Positive Airway Pressure(CPAP) treatment, which requires the patient to wear a mask throughwhich air is blown into the nostrils to keep the airway open. Othertreatment options include the implantation of rigid inserts in the softpalate to provide structural support, tracheotomies, or tissue ablation.

Another condition to which neural modulation may be applied is theoccurrence of migraine headaches. Pain sensation in the head istransmitted to the brain via the occipital nerve, specifically thegreater occipital nerve, and the trigeminal nerve. When a subjectexperiences head pain, such as during a migraine headache, theinhibition of these nerves may serve to decrease or eliminate thesensation of pain.

Neural modulation may also be applied to hypertension. Blood pressure inthe body is controlled via multiple feedback mechanisms. For example,baroreceptors in the carotid body in the carotid artery are sensitive toblood pressure changes within the carotid artery. The baroreceptorsgenerate signals that are conducted to the brain via theglossopharyngeal nerve when blood pressure rises, signaling the brain toactivate the body's regulation system to lower blood pressure, e.g.through changes to heart rate, and vasodilation/vasoconstriction.Conversely, parasympathetic nerve fibers on and around the renalarteries generate signals that are carried to the kidneys to initiateactions, such as salt retention and the release of angiotensin, whichraise blood pressure. Modulating these nerves may provide the ability toexert some external control over blood pressure.

The foregoing are just a few examples of conditions to whichneuromodulation may be of benefit, however embodiments of the inventiondescribed hereafter are not necessarily limited to treating only theabove-described conditions.

SUMMARY

A device for regulating energy delivery to an implanted circuit isdisclosed. The device according to some embodiments may include at leastone implantable circuit and at least one pair of implantable electrodesin electrical communication with the circuit. The at least oneimplantable circuit and at least one pair of implantable electrodes maybe configured for implantation in a vicinity of a genioglossus muscle ofa subject. The at least one pair of implantable electrodes may beconfigured to modulate a hypoglossal nerve. The at least one implantablecircuit may be configured deliver a power signal to the at least onepair of implantable electrodes. The power signal may have at least oneof a power level and a duration determined based on a severity of adetected physiologic condition.

The device according to some embodiments may include at least oneimplantable circuit and at least one pair of implantable electrodes inelectrical communication with the circuit. The at least one pair ofimplantable electrodes may be configured to modulate at least one nerve.The at least one implantable circuit may be configured deliver a powersignal to the at least one pair of implantable electrodes. The powersignal may have at least one of a power level and a duration determinedbased on a severity of a detected physiologic condition.

The device according to some embodiments may include a flexible carrierconfigured for implantation in a blood vessel of a subject, at least oneimplantable circuit, and at least one pair of implantable electrodes inelectrical communication with the circuit and located on the carrier.The at least one pair of implantable electrodes being configured tomodulate at least one of a renal nerve, a baroreceptor, and aglossopharyngeal nerve. The at least one implantable circuit may beconfigured deliver a power signal to the at least one pair ofimplantable electrodes. The power signal may have at least one of apower level and a duration determined based on a severity of a detectedphysiologic condition.

Some embodiments may include a method of regulating energy delivery toan implanted circuit for treating a sleep disordered breathingcondition. The method may include detecting a severity of aphysiological condition in a body of a subject and determining, based onthe severity of the physiological condition, at least one of a powerlevel or a duration of a power signal to be delivered by the implantedcircuit to at least one pair of electrodes implanted proximal to ahypoglossal nerve of the subject and in electrical communication withthe implanted circuit. The method may further include delivering thepower signal to the at least one pair of electrodes and the hypoglossalnerve of the subject via the power signal. The method may includedetermining a degree of coupling between a primary antenna associatedwith an external unit and a secondary antenna associated with an implantunit implanted in a body of a subject, and regulating delivery of powerto the implant unit based on the determined degree of coupling.

Additional features of the disclosure will be set forth in part in thedescription that follows, and in part will be obvious from thedescription, or may be learned by practice of the disclosed embodiments.

It is to be understood that both the foregoing general description andthe following detailed description are exemplary and explanatory only,and are not restrictive of the invention, as claimed.

BRIEF DESCRIPTION OF THE DRAWINGS

The accompanying drawings, which are incorporated in and constitute apart of this specification, illustrate several embodiments of thedisclosure and, together with the description, serve to explain theprinciples of the embodiments disclosed herein.

FIG. 1 schematically illustrates an implant unit and external unit,according to an exemplary embodiment of the present disclosure.

FIG. 2 is a partially cross-sectioned side view of a subject with animplant unit and external unit, according to an exemplary embodiment ofthe present disclosure.

FIG. 3 schematically illustrates a system including an implant unit andan external unit, according to an exemplary embodiment of the presentdisclosure.

FIG. 4 is a top view of an implant unit, according to an exemplaryembodiment of the present disclosure.

FIG. 5 is a top view of an alternate embodiment of an implant unit,according to an exemplary embodiment of the present disclosure.

FIG. 6 illustrates circuitry of an implant unit and an external unit,according to an exemplary embodiment of the present disclosure.

FIG. 7 illustrates a graph of quantities that may be used in determiningenergy delivery as a function coupling, according to an exemplarydisclosed embodiment.

FIG. 8 depicts a graph illustrating non-linear harmonics.

FIG. 9 depicts a graph of quantities that may be used in determiningenergy delivery as a function coupling, according to an exemplarydisclosed embodiment.

FIG. 10 depicts anatomy of the tongue and associated muscles and nerves.

FIG. 11 depicts an exemplary implant location for the treatment of sleepapnea.

FIG. 12 depicts an exemplary implant location for the treatment of headpain.

FIG. 13 depicts an exemplary implant location for the treatment ofhypertension.

FIG. 14 depicts an exemplary implant location for the treatment ofhypertension.

DESCRIPTION OF EXEMPLARY EMBODIMENTS

Reference will now be made in detail to exemplary embodiments of thepresent disclosure, examples of which are illustrated in theaccompanying drawings. Wherever possible, the same reference numberswill be used throughout the drawings to refer to the same or like parts.

Embodiments of the present disclosure relate generally to a device formodulating a nerve through the delivery of energy. Nerve modulation, orneural modulation, includes inhibition (e.g. blockage), stimulation,modification, regulation, or therapeutic alteration of activity,electrical or chemical, in the central, peripheral, or autonomic nervoussystem. Nerve modulation may take the form of nerve stimulation, whichmay include providing energy to the nerve to create a voltage changesufficient for the nerve to activate, or propagate an electrical signalof its own. Nerve modulation may also take the form of nerve inhibition,which may including providing energy to the nerve sufficient to preventthe nerve from propagating electrical signals. Nerve inhibition may beperformed through the constant application of energy, and may also beperformed through the application of enough energy to inhibit thefunction of the nerve for some time after the application. Other formsof neural modulation may modify the function of a nerve, causing aheightened or lessened degree of sensitivity. As referred to herein,modulation of a nerve may include modulation of an entire nerve and/ormodulation of a portion of a nerve. For example, modulation of a motorneuron may be performed to affect only those portions of the neuron thatare distal of the location to which energy is applied.

In patients with OSA, for example, a primary target response of nervestimulation may include contraction of a tongue muscle (e.g., themuscle) in order to move the tongue to a position that does not blockthe patient's airway. In the treatment of migraine headaches, nerveinhibition may be used to reduce or eliminate the sensation of pain. Inthe treatment of hypertension, neural modulation may be used toincrease, decrease, eliminate or otherwise modify nerve signalsgenerated by the body to regulate blood pressure.

While embodiments of the present disclosure may be disclosed for use inpatients with specific conditions, the embodiments may be used inconjunction with any patient/portion of a body where nerve modulationmay be desired. That is, in addition to use in patients with OSA,migraine headaches, or hypertension, embodiments of the presentdisclosure may be use in many other areas, including, but not limitedto: deep brain stimulation (e.g., treatment of epilepsy, Parkinson's,and depression); cardiac pace-making, stomach muscle stimulation (e.g.,treatment of obesity), back pain, incontinence, menstrual pain, and/orany other condition that may be affected by neural modulation.

FIG. 1 illustrates an implant unit and external unit, according to anexemplary embodiment of the present disclosure. An implant unit 110, maybe configured for implantation in a subject, in a location that permitsit to modulate a nerve 115. The implant unit 110 may be located in asubject such that intervening tissue 111 exists between the implant unit110 and the nerve 115. Intervening tissue may include muscle tissue,connective tissue, organ tissue, or any other type of biological tissue.Thus, location of implant unit 110 does not require contact with nerve115 for effective neuromodulation. The implant unit 110 may also belocated directly adjacent to nerve 115, such that no intervening tissue111 exists.

In treating OSA, implant unit 110 may be located on a genioglossusmuscle of a patient. Such a location is suitable for modulation of thehypoglossal nerve, branches of which run inside the genioglossus muscle.Further details regarding implantation locations of an implant unit 110for treatment of OSA are provided below with respect to FIGS. 10 and 11.Implant unit 110 may also be configured for placement in otherlocations. For example, migraine treatment may require subcutaneousimplantation in the back of the neck, near the hairline of a subject, orbehind the ear of a subject, to modulate the greater occipital nerve,lesser occipital nerve, and/or the trigeminal nerve. Further detailsregarding implantation locations of an implant unit 110 for treatment ofhead pain, such as migraine headaches, are provided below with respectto FIG. 12. Treating hypertension may require the implantation of aneuromodulation implant intravascularly inside the renal artery or renalvein (to modulate the parasympathetic renal nerves), either unilaterallyor bilaterally, inside the carotid artery or jugular vein (to modulatethe glossopharyngeal nerve through the carotid baroreceptors).Alternatively or additionally, treating hypertension may require theimplantation of a neuromodulation implant subcutaneously, behind the earor in the neck, for example, to directly modulate the glossopharyngealnerve. Further details regarding implantation locations of an implantunit 110 for treatment of hypertension are provided below, with respectto FIGS. 13 and 14.

External unit 120 may be configured for location external to a patient,either directly contacting, or close to the skin 112 of the patient.External unit 120 may be configured to be affixed to the patient, forexample, by adhering to the skin 112 of the patient, or through a bandor other device configured to hold external unit 120 in place. Adherenceto the skin of external unit 120 may occur such that it is in thevicinity of the location of implant unit 110.

FIG. 2 illustrates an exemplary embodiment of a neuromodulation systemfor delivering energy in a patient 100 with OSA. The system may includean external unit 120 that may be configured for location external to thepatient. As illustrated in FIG. 2, external unit 120 may be configuredto be affixed to the patient 100. FIG. 2 illustrates that in a patient100 with OSA, the external unit 120 may be configured for placementunderneath the patient's chin and/or on the front of patient's neck. Thesuitability of placement locations may be determined by communicationbetween external unit 120 and implant unit 110, discussed in greaterdetail below. In alternate embodiments, for the treatment of conditionsother than OSA, the external unit may be configured to be affixedanywhere suitable on a patient, such as the back of a patient's neck,i.e. for communication with a migraine treatment implant unit, on theouter portion of a patient's abdomen, i.e. for communication with astomach modulating implant unit, on a patient's back, i.e. forcommunication with a renal artery modulating implant unit, and/or on anyother suitable external location on a patient's skin, depending on therequirements of a particular application.

External unit 120 may further be configured to be affixed to analternative location proximate to the patient. For example, in oneembodiment, the external unit may be configured to fixedly or removablyadhere to a strap or a band that may be configured to wrap around a partof a patient's body. Alternatively, or in addition, the external unitmay be configured to remain in a desired location external to thepatient's body without adhering to that location.

The external unit 120 may include a housing. The housing may include anysuitable container configured for retaining components. In addition,while the external unit is illustrated schematically in FIG. 2, thehousing may be any suitable size and/or shape and may be rigid orflexible. Non-limiting examples of housings for the external unit 100include one or more of patches, buttons, or other receptacles havingvarying shapes and dimensions and constructed of any suitable material.In one embodiment, for example, the housing may include a flexiblematerial such that the external unit may be configured to conform to adesired location. For example, as illustrated in FIG. 2, the externalunit may include a skin patch, which, in turn, may include a flexiblesubstrate. The material of the flexible substrate may include, but isnot limited to, plastic, silicone, woven natural fibers, and othersuitable polymers, copolymers, and combinations thereof. Any portion ofexternal unit 120 may be flexible or rigid, depending on therequirements of a particular application.

As previously discussed, in some embodiments external unit 120 may beconfigured to adhere to a desired location. Accordingly, in someembodiments, at least one side of the housing may include an adhesivematerial. The adhesive material may include a biocompatible material andmay allow for a patient to adhere the external unit to the desiredlocation and remove the external unit upon completion of use. Theadhesive may be configured for single or multiple uses of the externalunit. Suitable adhesive materials may include, but are not limited tobiocompatible glues, starches, elastomers, thermoplastics, andemulsions.

FIG. 3 schematically illustrates a system including external unit 120and an implant unit 110. In some embodiments, internal unit 110 may beconfigured as a unit to be implanted into the body of a patient, andexternal unit 120 may be configured to send signals to and/or receivesignals from implant unit 110.

As shown in FIG. 3, various components may be included within a housingof external unit 120 or otherwise associated with external unit 120. Asillustrated in FIG. 3, at least one processor 144 may be associated withexternal unit 120. For example, the at least one processor 144 may belocated within the housing of external unit 120. In alternativeembodiments, the at least one processor may be configured for wired orwireless communication with the external unit from a location externalto the housing.

The at least one processor may include any electric circuit that may beconfigured to perform a logic operation on at least one input variable.The at least one processor may therefore include one or more integratedcircuits, microchips, microcontrollers, and microprocessors, which maybe all or part of a central processing unit (CPU), a digital signalprocessor (DSP), a field programmable gate array (FPGA), or any othercircuit known to those skilled in the art that may be suitable forexecuting instructions or performing logic operations.

FIG. 3 illustrates that the external unit 120 may further be associatedwith a power source 140. The power source may be removably couplable tothe external unit at an exterior location relative to external unit.Alternatively, as shown in FIG. 3, power source 140 may be permanentlyor removably coupled to a location within external unit 120. The powersource may further include any suitable source of power configured to bein electrical communication with the processor. In one embodiment, forexample the power source 140 may include a battery.

The power source may be configured to power various components withinthe external unit. As illustrated in FIG. 3, power source 140 may beconfigured to provide power to the processor 144. In addition, the powersource 140 may be configured to provide power to a signal source 142.The signal source 142 may be in communication with the processor 144 andmay include any device configured to generate a signal (e.g., asinusoidal signal, square wave, triangle wave, microwave,radio-frequency (RF) signal, or any other type of electromagneticsignal). Signal source 142 may include, but is not limited to, awaveform generator that may be configured to generate alternatingcurrent (AC) signals and/or direct current (DC) signals. In oneembodiment, for example, signal source 142 may be configured to generatean AC signal for transmission to one or more other components. Signalsource 142 may be configured to generate a signal of any suitablefrequency. In some embodiments, signal source 142 may be configured togenerate a signal having a frequency of from about 6.5 MHz to about 13.6MHz. In additional embodiments, signal source 142 may be configured togenerate a signal having a frequency of from about 7.4 to about 8.8 MHz.In further embodiments, signal source 142 may generate a signal having afrequency as low as 90 kHz or as high as 28 MHz.

Signal source 142 may be configured for direct or indirect electricalcommunication with an amplifier 146. The amplifier may include anysuitable device configured to amplify one or more signals generated fromsignal source 142. Amplifier 146 may include one or more of varioustypes of amplification devices, including, for example, transistor baseddevices, operational amplifiers, RF amplifiers, power amplifiers, or anyother type of device that can increase the gain associated one or moreaspects of a signal. The amplifier may further be configured to outputthe amplified signals to one or more components within external unit120.

The external unit may additionally include a primary antenna 150. Theprimary antenna may be configured as part of a circuit within externalunit 120 and may be coupled either directly or indirectly to variouscomponents in external unit 120. For example, as shown in FIG. 3,primary antenna 150 may be configured for communication with theamplifier 146.

The primary antenna may include any conductive structure that may beconfigured to create an electromagnetic field. The primary antenna mayfurther be of any suitable size, shape, and/or configuration. The size,shape, and/or configuration may be determined by the size of thepatient, the placement location of the implant unit, the size and/orshape of the implant unit, the amount of energy required to modulate anerve, a location of a nerve to be modulated, the type of receivingelectronics present on the implant unit, etc. The primary antenna mayinclude any suitable antenna known to those skilled in the art that maybe configured to send and/or receive signals. Suitable antennas mayinclude, but are not limited to, a long-wire antenna, a patch antenna, ahelical antenna, etc. In one embodiment, for example, as illustrated inFIG. 3, primary antenna 150 may include a coil antenna. Such a coilantenna may be made from any suitable conductive material and may beconfigured to include any suitable arrangement of conductive coils(e.g., diameter, number of coils, layout of coils, etc.). A coil antennasuitable for use as primary antenna 150 may have a diameter of betweenabout 1 cm and 10 cm, and may be circular or oval shaped. In someembodiments, a coil antenna may have a diameter between 5 cm and 7 cm,and may be oval shaped. A coil antenna suitable for use as primaryantenna 150 may have any number of windings, e.g. 4, 8, 12, or more. Acoil antenna suitable for use as primary antenna 150 may have a wirediameter between about 0.1 mm and 2 mm. These antenna parameters areexemplary only, and may be adjusted above or below the ranges given toachieve suitable results.

As noted, implant unit 110 may be configured to be implanted in apatient's body (e.g., beneath the patient's skin). FIG. 2 illustratesthat the implant unit 110 may be configured to be implanted formodulation of a nerve associated with a muscle of the subject's tongue130. Modulating a nerve associated with a muscle of the subject's tongue130 may include stimulation to cause a muscle contraction. In furtherembodiments, the implant unit may be configured to be placed inconjunction with any nerve that one may desire to modulate. For example,modulation of the occipital nerve, the greater occipital nerve, and/orthe trigeminal nerve may be useful for treating pain sensation in thehead, such as that from migraines. Modulation of parasympathetic nervefibers on and around the renal arteries (i.e.. the renal nerves), thevagus nerve, and /or the glossopharyngeal nerve may be useful fortreating hypertension. Additionally, any nerve of the peripheral nervoussystem (both spinal and cranial), including motor neurons, sensoryneurons, sympathetic neurons and parasympathetic neurons, may bemodulated to achieve a desired effect.

Implant unit 110 may be formed of any materials suitable forimplantation into the body of a patient. In some embodiments, implantunit 110 may include a flexible carrier 161 (FIG. 4) including aflexible, biocompatible material. Such materials may include, forexample, silicone, polyimides, phenyltrimethoxysilane (PTMS), polymethylmethacrylate (PMMA), Parylene C, polyimide, liquid polyimide, laminatedpolyimide, black epoxy, polyether ether ketone (PEEK), Liquid CrystalPolymer (LCP), Kapton, etc. Implant unit 110 may further includecircuitry including conductive materials, such as gold, platinum,titanium, or any other biocompatible conductive material or combinationof materials. Implant unit 110 and flexible carrier 161 may also befabricated with a thickness suitable for implantation under a patient'sskin. Implant 110 may have thickness of less than about 4 mm or lessthan about 2 mm.

Other components that may be included in or otherwise associated withthe implant unit are illustrated in FIG. 3. For example, implant unit110 may include a secondary antenna 152 mounted onto or integrated withflexible carrier 161. Similar to the primary antenna, the secondaryantenna may include any suitable antenna known to those skilled in theart that may be configured to send and/or receive signals. The secondaryantenna may include any suitable size, shape, and/or configuration. Thesize, shape and/or configuration may be determined by the size of thepatient, the placement location of the implant unit, the amount ofenergy required to modulate the nerve, etc. Suitable antennas mayinclude, but are not limited to, a long-wire antenna, a patch antenna, ahelical antenna, etc. In some embodiments, for example, secondaryantenna 152 may include a coil antenna having a circular shape (see alsoFIG. 4) or oval shape. Such a coil antenna may be made from any suitableconductive material and may be configured to include any suitablearrangement of conductive coils (e.g., diameter, number of coils, layoutof coils, etc.). A coil antenna suitable for use as secondary antenna152 may have a diameter of between about 5 mm and 30 mm, and may becircular or oval shaped. A coil antenna suitable for use as secondaryantenna 152 may have any number of windings, e.g. 4, 15, 20, 30, or 50.A coil antenna suitable for use as secondary antenna 152 may have a wirediameter between about 0.01 mm and 1 mm. These antenna parameters areexemplary only, and may be adjusted above or below the ranges given toachieve suitable results.

Implant unit 110 may additionally include a plurality offield-generating implant electrodes 158 a, 158 b. The electrodes mayinclude any suitable shape and/or orientation on the implant unit solong as the electrodes may be configured to generate an electric fieldin the body of a patient. Implant electrodes 158 a and 158 b may alsoinclude any suitable conductive material (e.g., copper, silver, gold,platinum, iridium, platinum-iridium, platinum-gold, conductive polymers,etc.) or combinations of conductive (and/or noble metals) materials. Insome embodiments, for example, the electrodes may include short lineelectrodes, circular electrodes, and/or circular pairs of electrodes. Asshown in FIG. 4, electrodes 158 a and 158 b may be located on an end ofa first extension 162 a of an elongate arm 162. The electrodes, however,may be located on any portion of implant unit 110. Additionally, implantunit 110 may include electrodes located at a plurality of locations, forexample on an end of both a first extension 162 a and a second extension162 b of elongate arm 162, as illustrated, for example, in FIG. 5.Implant electrodes may have a thickness between about 200 nanometers and1 millimeter. Anode and cathode electrode pairs may be spaced apart byabout a distance of about 0.2 mm to 25 mm. In additional embodiments,anode and cathode electrode pairs may be spaced apart by a distance ofabout 1 mm to 10 mm, or between 4 mm and 7 mm. Adjacent anodes oradjacent cathodes may be spaced apart by distances as small as 0.001 mmor less, or as great as 25 mm or more. In some embodiments, adjacentanodes or adjacent cathodes may be spaced apart by a distance betweenabout 0.2 mm and 1 mm.

FIG. 4 provides a schematic representation of an exemplary configurationof implant unit 110. As illustrated in FIG. 4, in one embodiment, thefield-generating electrodes 158 a and 158 b may include two sets of fourcircular electrodes, provided on flexible carrier 161, with one set ofelectrodes providing an anode and the other set of electrodes providinga cathode. Implant unit 110 may include one or more structural elementsto facilitate implantation of implant unit 110 into the body of apatient. Such elements may include, for example, elongated arms, sutureholes, polymeric surgical mesh, biological glue, spikes of flexiblecarrier protruding to anchor to the tissue, spikes of additionalbiocompatible material for the same purpose, etc. that facilitatealignment of implant unit 110 in a desired orientation within apatient's body and provide attachment points for securing implant unit110 within a body. For example, in some embodiments, implant unit 110may include an elongate arm 162 having a first extension 162 a and,optionally, a second extension 162 b. Extensions 162 a and 162 b may aidin orienting implant unit 110 with respect to a particular muscle (e.g.,the genioglossus muscle), a nerve within a patient's body, or a surfacewithin a body above a nerve. For example, first and second extensions162 a, 162 b may be configured to enable the implant unit to conform atleast partially around soft or hard tissue (e.g., nerve, bone, ormuscle, etc.) beneath a patient's skin. Further, implant unit 110 mayalso include one or more suture holes 160 located anywhere on flexiblecarrier 161. For example, in some embodiments, suture holes 160 may beplaced on second extension 162 b of elongate arm 162 and/or on firstextension 162 a of elongate arm 162. Implant unit 110 may be constructedin various shapes. In some embodiments, implant unit may appearsubstantially as illustrated in FIG. 4. In other embodiments, implantunit 110 may lack illustrated structures such as second extension 162 b,or may have additional or different structures in differentorientations. Additionally, implant unit 110 may be formed with agenerally triangular, circular, or rectangular shape, as an alternativeto the winged shape shown in FIG. 4. In some embodiments, the shape ofimplant unit 110 (e.g., as shown in FIG. 4) may facilitate orientationof implant unit 110 with respect to a particular nerve to be modulated.Thus, other regular or irregular shapes may be adopted in order tofacilitate implantation in differing parts of the body.

As illustrated in FIG. 4, secondary antenna 152 and electrodes 158 a,158 b may be mounted on or integrated with flexible carrier 161. Variouscircuit components and connecting wires (discussed further below) may beused to connect secondary antenna with implant electrodes 158 a and 158b. To protect the antenna, electrodes, circuit components, andconnecting wires from the environment within a patient's body, implantunit 110 may include a protective coating that encapsulates implant unit110. In some embodiments, the protective coating may be made from aflexible material to enable bending along with flexible carrier 161. Theencapsulation material of the protective coating may also resisthumidity penetration and protect against corrosion. In some embodiments,the protective coating may include silicone, polyimides,phenyltrimethoxysilane (PTMS), polymethyl methacrylate (PMMA), ParyleneC, liquid polyimide, laminated polyimide, polyimide, Kapton, blackepoxy, polyether ketone (PEEK), Liquid Crystal Polymer (LCP), or anyother suitable biocompatible coating. In some embodiments, theprotective coating may include a plurality of layers, includingdifferent materials or combinations of materials in different layers.

FIG. 5 is a perspective view of an alternate embodiment of an implantunit 110, according to an exemplary embodiment of the presentdisclosure. As illustrated in FIG. 5, implant unit 110 may include aplurality of electrodes, located, for example, at the ends of firstextension 162 a and second extension 162 b. FIG. 5 illustrates anembodiment wherein implant electrodes 158 a and 158 b include short lineelectrodes.

Returning to FIGS. 2 and 3, external unit 120 may be configured tocommunicate with implant unit 110. For example, in some embodiments, aprimary signal may be generated on primary antenna 150, using, e.g.,processor 144, signal source 142, and amplifier 146. More specifically,in one embodiment, power source 140 may be configured to provide powerto one or both of the processor 144 and the signal source 142. Theprocessor 144 may be configured to cause signal source 142 to generate asignal (e.g., an RF energy signal). Signal source 142 may be configuredto output the generated signal to amplifier 146, which may amplify thesignal generated by signal source 142. The amount of amplification and,therefore, the amplitude of the signal may be controlled, for example,by processor 144. The amount of gain or amplification that processor 144causes amplifier 146 to apply to the signal may depend on a variety offactors, including, but not limited to, the shape, size, and/orconfiguration of primary antenna 150, the size of the patient, thelocation of implant unit 110 in the patient, the shape, size, and/orconfiguration of secondary antenna 152, a degree of coupling betweenprimary antenna 150 and secondary antenna 152 (discussed further below),a desired magnitude of electric field to be generated by implantelectrodes 158 a, 158 b, etc. Amplifier 146 may output the amplifiedsignal to primary antenna 150.

External unit 120 may communicate a primary signal on primary antenna tothe secondary antenna 152 of implant unit 110. This communication mayresult from coupling between primary antenna 150 and secondary antenna152. Such coupling of the primary antenna and the secondary antenna mayinclude any interaction between the primary antenna and the secondaryantenna that causes a signal on the secondary antenna in response to asignal applied to the primary antenna. In some embodiments, couplingbetween the primary and secondary antennas may include capacitivecoupling, inductive coupling, radiofrequency coupling, etc. and anycombinations thereof.

Coupling between primary antenna 150 and secondary antenna 152 maydepend on the proximity of the primary antenna relative to the secondaryantenna. That is, in some embodiments, an efficiency or degree ofcoupling between primary antenna 150 and secondary antenna 152 maydepend on the proximity of the primary antenna to the secondary antenna.The proximity of the primary and secondary antennas may be expressed interms of a coaxial offset (e.g., a distance between the primary andsecondary antennas when central axes of the primary and secondaryantennas are co-aligned), a lateral offset (e.g., a distance between acentral axis of the primary antenna and a central axis of the secondaryantenna), and/or an angular offset (e.g., an angular difference betweenthe central axes of the primary and secondary antennas). In someembodiments, a theoretical maximum efficiency of coupling may existbetween primary antenna 150 and secondary antenna 152 when both thecoaxial offset, the lateral offset, and the angular offset are zero.Increasing any of the coaxial offset, the lateral offset, and theangular offset may have the effect of reducing the efficiency or degreeof coupling between primary antenna 150 and secondary antenna 152.

As a result of coupling between primary antenna 150 and secondaryantenna 152, a secondary signal may arise on secondary antenna 152 whenthe primary signal is present on the primary antenna 150. Such couplingmay include inductive/magnetic coupling, RF coupling/transmission,capacitive coupling, or any other mechanism where a secondary signal maybe generated on secondary antenna 152 in response to a primary signalgenerated on primary antenna 150. Coupling may refer to any interactionbetween the primary and secondary antennas. In addition to the couplingbetween primary antenna 150 and secondary antenna 152, circuitcomponents associated with implant unit 110 may also affect thesecondary signal on secondary antenna 152. Thus, the secondary signal onsecondary antenna 152 may refer to any and all signals and signalcomponents present on secondary antenna 152 regardless of the source.

While the presence of a primary signal on primary antenna 150 may causeor induce a secondary signal on secondary antenna 152, the couplingbetween the two antennas may also lead to a coupled signal or signalcomponents on the primary antenna 150 as a result of the secondarysignal present on secondary antenna 152. A signal on primary antenna 150induced by a secondary signal on secondary antenna 152 may be referredto as a primary coupled signal component. The primary signal may referto any and all signals or signal components present on primary antenna150, regardless of source, and the primary coupled signal component mayrefer to any signal or signal component arising on the primary antennaas a result of coupling with signals present on secondary antenna 152.Thus, in some embodiments, the primary coupled signal component maycontribute to the primary signal on primary antenna 150.

Implant unit 110 may be configured to respond to external unit 120. Forexample, in some embodiments, a primary signal generated on primary coil150 may cause a secondary signal on secondary antenna 152, which inturn, may cause one or more responses by implant unit 110. In someembodiments, the response of implant unit 110 may include the generationof an electric field between implant electrodes 158 a and 158 b.

FIG. 6 illustrates circuitry 170 that may be included in external unit120 and circuitry 180 that may be included in implant unit 110.Additional, different, or fewer circuit components may be included ineither or both of circuitry 170 and circuitry 180. As shown in FIG. 6,secondary antenna 152 may be arranged in electrical communication withimplant electrodes 158 a, 158 b. In some embodiments, circuitryconnecting secondary antenna 152 with implant electrodes 158 a and 158 bmay cause a voltage potential across implant electrodes 158 a and 158 bin the presence of a secondary signal on secondary antenna 152. Thisvoltage potential may be referred to as a field inducing signal, as thisvoltage potential may generate an electric field between implantelectrodes 158 a and 158 b. More broadly, the field inducing signal mayinclude any signal (e.g., voltage potential) applied to electrodesassociated with the implant unit that may result in an electric fieldbeing generated between the electrodes.

The field inducing signal may be generated as a result of conditioningof the secondary signal by circuitry 180. As shown in FIG. 6, circuitry170 of external unit 120 may be configured to generate an AC primarysignal on primary antenna 150 that may cause an AC secondary signal onsecondary antenna 152. In certain embodiments, however, it may beadvantageous (e.g., in order to generate a unidirectional electric fieldfor modulation of a nerve) to provide a DC field inducing signal atimplant electrodes 158 a and 158 b. To convert the AC secondary signalon secondary antenna 152 to a DC field inducing signal, circuitry 180 inimplant unit 110 may include a signal modifier, for example, an AC-DCconverter. The AC to DC converter may include any suitable converterknown to those skilled in the art. For example, in some embodiments theAC-DC converter may include rectification circuit components including,for example, diode 156 and appropriate capacitors and resistors. Inalternative embodiments, implant unit 110 may include an AC-ACconverter, or no converter, in order to provide an AC field inducingsignal at implant electrodes 158 a and 158 b.

As noted above, the field inducing signal may be configured to generatean electric field between implant electrodes 158 a and 158 b. In someinstances, the magnitude and/or duration of the generated electric fieldresulting from the field inducing signal may be sufficient to modulateone or more nerves in the vicinity of electrodes 158 a and 158 b. Insuch cases, the field inducing signal may be referred to as a modulationsignal. In other instances, the magnitude and/or duration of the fieldinducing signal may generate an electric field that does not result innerve modulation. In such cases, the field inducing signal may bereferred to as a sub-modulation signal.

Various types of field inducing signals may constitute modulationsignals. For example, in some embodiments, a modulation signal mayinclude a moderate amplitude and moderate duration, while in otherembodiments, a modulation signal may include a higher amplitude and ashorter duration. Various amplitudes and/or durations of field-inducingsignals across electrodes 158 a, 158 b may result in modulation signals,and whether a field-inducing signal rises to the level of a modulationsignal can depend on many factors (e.g., distance from a particularnerve to be stimulated; whether the nerve is branched; orientation ofthe induced electric field with respect to the nerve; type of tissuepresent between the electrodes and the nerve; etc.).

Whether a field inducing signal constitutes a modulation signal(resulting in an electric field that may cause nerve modulation) or asub-modulation signal (resulting in an electric field not intended tocause nerve modulation) may ultimately be controlled by processor 144 ofexternal unit 120. For example, in certain situations, processor 144 maydetermine that nerve modulation is appropriate. Under these conditions,processor 144 may cause signal source 144 and amplifier 146 to generatea modulation control signal on primary antenna 150 (i.e., a signalhaving a magnitude and/or duration selected such that a resultingsecondary signal on secondary antenna 152 will provide a modulationsignal at implant electrodes 158 a and 158 b).

Processor 144 may be configured to limit an amount of energy transferredfrom external unit 120 to implant unit 110. For example, in someembodiments, implant unit 110 may be associated with a threshold energylimit that may take into account multiple factors associated with thepatient and/or the implant. For example, in some cases, certain nervesof a patient should receive no more than a predetermined maximum amountof energy to minimize the risk of damaging the nerves and/or surroundingtissue. Additionally, circuitry 180 of implant unit 110 may includecomponents having a maximum operating voltage or power level that maycontribute to a practical threshold energy limit of implant unit 110.For example, components including diodes may be included in implant unit110 or in external unit 120 to limit power transferred from the externalunit 120 to the implant unit 110. In some embodiments, diode 156 mayfunction to limit the power level received by the patient. Processor 144may be configured to account for such limitations when setting themagnitude and/or duration of a primary signal to be applied to primaryantenna 150.

In addition to determining an upper limit of power that may be deliveredto implant unit 110, processor 144 may also determine a lower powerthreshold based, at least in part, on an efficacy of the deliveredpower. The lower power threshold may be computed based on a minimumamount of power that enables nerve modulation (e.g., signals havingpower levels above the lower power threshold may constitute modulationsignals while signals having power levels below the lower powerthreshold may constitute sub-modulation signals).

A lower power threshold may also be measured or provided in alternativeways. For example, appropriate circuitry or sensors in the implant unit110 may measure a lower power threshold. A lower power threshold may becomputed or sensed by an additional external device, and subsequentlyprogrammed into processor 144, or programmed into implant unit 110.Alternatively, implant unit 110 may be constructed with circuitry 180specifically chosen to generate signals at the electrodes of at leastthe lower power threshold. In still another embodiment, an antenna ofexternal unit 120 may be adjusted to accommodate or produce a signalcorresponding to a specific lower power threshold. The lower powerthreshold may vary from patient to patient, and may take into accountmultiple factors, such as, for example, modulation characteristics of aparticular patient's nerve fibers, a distance between implant unit 110and external unit 120 after implantation, and the size and configurationof implant unit components (e.g., antenna and implant electrodes), etc.

Processor 144 may also be configured to cause application ofsub-modulation control signals to primary antenna 150. Suchsub-modulation control signals may include an amplitude and/or durationthat result in a sub-modulation signal at electrodes 158 a, 158 b. Whilesuch sub-modulation control signals may not result in nerve modulation,such sub-modulation control signals may enable feedback-based control ofthe nerve modulation system. That is, in some embodiments, processor 144may be configured to cause application of a sub-modulation controlsignal to primary antenna 150. This signal may induce a secondary signalon secondary antenna 152, which, in turn, induces a primary coupledsignal component on primary antenna 150.

To analyze the primary coupled signal component induced on primaryantenna 150, external unit 120 may include a feedback circuit 148 (e.g.,a signal analyzer or detector, etc.), which may be placed in direct orindirect communication with primary antenna 150 and processor 144.Sub-modulation control signals may be applied to primary antenna 150 atany desired periodicity. In some embodiments, the sub-modulation controlsignals may be applied to primary antenna 150 at a rate of one everyfive seconds (or longer). In other embodiments, the sub-modulationcontrol signals may be applied more frequently (e.g., once every twoseconds, once per second, once per millisecond, once per nanosecond, ormultiple times per second). Further, it should be noted that feedbackmay also be received upon application of modulation control signals toprimary antenna 150 (i.e., those that result in nerve modulation), assuch modulation control signals may also result in generation of aprimary coupled signal component on primary antenna 150.

The primary coupled signal component may be fed to processor 144 byfeedback circuit 148 and may be used as a basis for determining a degreeof coupling between primary antenna 150 and secondary antenna 152.Measuring the degree of coupling may enable determination of theefficacy of the energy transfer between two antennas. Processor 144 mayalso use the determined degree of coupling in regulating delivery ofpower to implant unit 110.

Processor 144 may be configured with any suitable logic for determininghow to regulate power transfer to implant unit 110 based on thedetermined degree of coupling. .Processor 144 may, for example, utilizea baseline coupling range. Presumably, while the patient is awake, thetongue is not blocking the patient's airway and moves with the patient'sbreathing in a natural range, where coupling between primary antenna 150and secondary antenna 152 may be within a baseline coupling range. Abaseline coupling range may encompass a maximum coupling between primaryantenna 150 and secondary antenna 152. A baseline coupling range mayalso encompass a range that does not include a maximum coupling levelbetween primary antenna 150 and secondary antenna 152. Processor 144 maybe configured to determine the baseline coupling range based on acommand from a user, such as the press of a button on the patch or thepress of a button on a suitable remote device. Alternatively oradditionally, processor 144 may be configured to automatically determinethe baseline coupling range when external unit 120 is placed such thatprimary antenna 150 and secondary antenna 152 are within range of eachother. In such an embodiment, when processor 144 detects any degree ofcoupling between primary antenna 150 and secondary antenna 152, it mayimmediately begin tracking a baseline coupling range. Processor 144 maythen determine a baseline coupling range when it detects that the onlymovement between primary antenna 150 and secondary antenna 152 is causedby a patient's natural breathing rhythm (i.e., the patient has securedthe external unit to an appropriate location on their body).Additionally, processor 144 may be configured such that it measurescoupling between the primary antenna 150 and the secondary antenna 152for a specified period of time after activation in order to determine abaseline coupling range, such as 1 minute, 5 minutes, 10 minutes, etc.

Where the primary coupled signal component indicates that a degree ofcoupling has changed from a baseline coupling range, processor 144 maydetermine that secondary antenna 152 has moved with respect to primaryantenna 150 (either in coaxial offset, lateral offset, or angularoffset, or any combination). Such movement, for example, may beassociated with a movement of the implant unit 110, and the tissue thatit is associated with based on its implant location. Thus, in suchsituations, processor 144 may determine that modulation of a nerve inthe patient's body is appropriate. More particularly, in response to anindication of a change in coupling, processor 144, in some embodiments,may cause application of a modulation control signal to primary antenna150 in order to generate a modulation signal at implant electrodes 158a, 158 b, e.g., to cause modulation of a nerve of the patient.

In an embodiment for the treatment of OSA, movement of an implant unit110 may be associated with movement of the tongue, which may indicatethe onset of a sleep apnea event or a sleep apnea precursor. The onsetof a sleep apnea event of sleep apnea precursor may require thestimulation of the genioglossus muscle of the patient to relieve oravert the event. Such stimulation may result in contraction of themuscle and movement of the patient's tongue away from the patient'sairway.

In embodiments for the treatment of head pain, including migraines,processor 144 may be configured to generate a modulation control signalbased on a signal from a user, for example, or a detected level ofneural activity in a sensory neuron (e.g. the greater occipital nerve ortrigeminal nerve) associated with head pain. A modulation control signalgenerated by the processor and applied to the primary antenna 150 maygenerate a modulation signal at implant electrodes 158 a, 158 b, e.g.,to cause inhibition or blocking (i.e. a down modulation) of a sensorynerve of the patient. Such inhibition or blocking may decrease oreliminate the sensation of pain for the patient.

In embodiments for the treatment of hypertension, processor 144 may beconfigured to generate a modulation control signal based on, forexample, pre-programmed instructions and/or signals from an implantindicative of blood pressure. A modulation control signal generated bythe processor and applied to the primary antenna 150 may generate amodulation signal at implant electrodes 158 a, 158 b, e.g., to causeeither inhibition or stimulation of nerve of a patient, depending on therequirements. For example, a neuromodulator placed in a carotid arteryor jugular vein (i.e. in the vicinity of a carotid baroreceptor), mayreceive a modulation control signal tailored to induce a stimulationsignal at the electrodes, thereby causing the glossopharyngeal nerveassociated with the carotid baroreceptors to fire at an increased ratein order to signal the brain to lower blood pressure. Similar modulationof the glossopharyngeal nerve may be achieved with a neuromodulatorimplanted in a subcutaneous location in a patient's neck or behind apatient's ear. A neuromodulator place in a renal artery may receive amodulation control signal tailored to cause an inhibiting or blockingsignal (i.e. a down modulation) at the electrodes, thereby inhibiting asignal to raise blood pressure carried from the renal nerves to thekidneys.

Modulation control signals may include stimulation control signals, andsub-modulation control signals may include sub-stimulation controlsignals. Stimulation control signals may have any amplitude, pulseduration, or frequency combination that results in a stimulation signalat electrodes 158 a, 158 b. In some embodiments (e.g., at a frequency ofbetween about 6.5-13.6 MHz), stimulation control signals may include apulse duration of greater than about 50 microseconds and/or an amplitudeof approximately 0.5 amps, or between 0.1 amps and 1 amp, or between0.05 amps and 3 amps. Sub-stimulation control signals may have a pulseduration less than about 500, or less than about 200 nanoseconds and/oran amplitude less than about 1 amp, 0.5 amps, 0.1 amps, 0.05 amps, or0.01 amps. Of course, these values are meant to provide a generalreference only, as various combinations of values higher than or lowerthan the exemplary guidelines provided may or may not result in nervestimulation.

In some embodiments, stimulation control signals may include a pulsetrain, wherein each pulse includes a plurality of sub-pulses. Analternating current signal (e.g., at a frequency of between about6.5-13.6 MHz) may be used to generate the pulse train, as follows. Asub-pulse may have a duration of between 50-250 microseconds, or aduration of between 1 microsecond and 2 milliseconds, during which analternating current signal is turned on. For example, a 200 microsecondsub-pulse of a 10 MHz alternating current signal will includeapproximately 2000 periods. Each pulse may, in turn, have a duration ofbetween 100 and 500 milliseconds, during which sub-pulses occur at afrequency of between 25 and 100 Hz. For example, a 200 millisecond pulseof 50 Hz sub-pulses will include approximately 10 sub-pulses. Finally,in a pulse train, each pulse may be separated from the next by aduration of between 0.2 and 2 seconds. For example, in a pulse train of200 millisecond pulses, each separated by 1.3 seconds from the next, anew pulse will occur every 1.5 seconds. A pulse train of this embodimentmay be utilized, for example, to provide ongoing stimulation during atreatment session. In the context of OSA, a treatment session may be aperiod of time during which a subject is asleep and in need of treatmentto prevent OSA. Such a treatment session may last anywhere from aboutthree to ten hours. In the context of other conditions to which neuralmodulators of the present disclosure are applied, a treatment sessionmay be of varying length according to the duration of the treatedcondition.

Processor 144 may be configured to determine a degree of couplingbetween primary antenna 150 and secondary antenna 152 by monitoring oneor more aspects of the primary coupled signal component received throughfeedback circuit 148. In some embodiments, processor 144 may determine adegree of coupling between primary antenna 150 and secondary antenna 152by monitoring a voltage level associated with the primary coupled signalcomponent, a current level, or any other attribute that may depend onthe degree of coupling between primary antenna 150 and secondary antenna152. For example, in response to periodic sub-modulation signals appliedto primary antenna 150, processor 144 may determine a baseline voltagelevel or current level associated with the primary coupled signalcomponent. This baseline voltage level, for example, may be associatedwith a range of movement of the patient's tongue when a sleep apneaevent or its precursor is not occurring, e.g. during normal breathing.As the patient's tongue moves toward a position associated with a sleepapnea event, moves in a manner consistent with a precursor of sleepapnea, or moves in any other manner (e.g., vibration, etc.), thecoaxial, lateral, or angular offset between primary antenna 150 andsecondary antenna 152 may change. As a result, the degree of couplingbetween primary antenna 150 and secondary antenna 152 may change, andthe voltage level or current level of the primary coupled signalcomponent on primary antenna 150 may also change. Processor 144 may beconfigured to recognize a sleep apnea event or its precursor when avoltage level, current level, or other electrical characteristicassociated with the primary coupled signal component changes by apredetermined amount or reaches a predetermined absolute value.

FIG. 7 provides a graph that illustrates this principle in more detail.For a two-coil system where one coil receives a radio frequency (RF)drive signal, graph 200 plots a rate of change in induced current in thereceiving coil as a function of coaxial distance between the coils. Forvarious coil diameters and initial displacements, graph 200 illustratesthe sensitivity of the induced current to further displacement betweenthe coils, moving them either closer together or further apart. It alsoindicates that, overall, the induced current in the secondary coil willdecrease as the secondary coil is moved away from the primary, drivecoil, i.e. the rate of change of induced current, in mA/mm, isconsistently negative. The sensitivity of the induced current to furtherdisplacement between the coils varies with distance. For example, at aseparation distance of 10 mm, the rate of change in current as afunction of additional displacement in a 14 mm coil is approximately −6mA/mm. If the displacement of the coils is approximately 22 mm, the rateof change in the induced current in response to additional displacementis approximately −11 mA/mm, which corresponds to a local maximum in therate of change of the induced current. Increasing the separationdistance beyond 22 mm continues to result in a decline in the inducedcurrent in the secondary coil, but the rate of change decreases. Forexample, at a separation distance of about 30 mm, the 14 mm coilexperiences a rate of change in the induced current in response toadditional displacement of about −8 mA/mm. With this type ofinformation, processor 144 may be able to determine a particular degreeof coupling between primary antenna 150 and secondary antenna 152, atany given time, by observing the magnitude and/or rate of change in themagnitude of the current associated with the primary coupled signalcomponent on primary antenna 150.

Processor 144 may be configured to determine a degree of couplingbetween primary antenna 150 and secondary antenna 152 by monitoringother aspects of the primary coupled signal component. For example, insome embodiments, the non-linear behavior of circuitry 180 in implantunit 110 may be monitored to determine a degree of coupling. Forexample, the presence, absence, magnitude, reduction and/or onset ofharmonic components in the primary coupled signal component on primaryantenna 150 may reflect the behavior of circuitry 180 in response tovarious control signals (either sub-modulation or modulation controlsignals) and, therefore, may be used to determine a degree of couplingbetween primary antenna 150 and secondary antenna 152.

As shown in FIG. 6, circuitry 180 in implant unit 110 may constitute anon-linear circuit due, for example, to the presence of non-linearcircuit components, such as diode 156. Such non-linear circuitcomponents may induce non-linear voltage responses under certainoperation conditions. Non-linear operation conditions may be inducedwhen the voltage potential across diode 156 exceeds the activationthreshold for diode 156. Thus, when implant circuitry 180 is excited ata particular frequency, this circuit may oscillate (or harmonicallyresonate) at multiple frequencies. The harmonic resonance may besymmetric or asymmetric. Spectrum analysis of the secondary signal onsecondary antenna 152, therefore, may reveal one or more oscillations,called harmonics, that appear at certain multiples of the excitationfrequency. Through coupling of primary antenna 150 and secondary antenna152, any harmonics produced by implant circuitry 180 and appearing onsecondary antenna 152 may also appear in the primary coupled signalcomponent present on primary antenna 150.

In certain embodiments, circuitry 180 may include additional circuitcomponents that alter the characteristics of the harmonics generated incircuitry 180 above a certain transition point. Monitoring how thesenon-linear harmonics behave above and below the transition point mayenable a determination of a degree of coupling between primary antenna150 and secondary antenna 152. For example, as shown in FIG. 6,circuitry 180 may include a harmonics modifier circuit 154, which mayinclude any electrical components that non-linearly alter the harmonicsgenerated in circuitry 180. In some embodiments, harmonics modifiercircuit 154 may include a pair of Zener diodes. Below a certain voltagelevel, these Zener diodes remain forward biased such that no currentwill flow through either diode. Above the breakdown voltage of the Zenerdiodes, however, these devices become conductive in the reversed biaseddirection and will allow current to flow through harmonics modifiercircuit 154. Once the Zener diodes become conductive, they begin toaffect the oscillatory behavior of circuitry 180, and, as a result,certain harmonic oscillation frequencies may be affected (e.g., reducedin magnitude).

FIGS. 8 and 9 illustrate this effect. For example, FIG. 8 illustrates agraph 300 a that shows the oscillatory behavior of circuitry 180 atseveral amplitudes ranging from about 10 nanoamps to about 20 microamps.As shown, the primary excitation frequency occurs at about 6.7 MHz andharmonics appear both at even and odd multiples of the primaryexcitation frequency. For example, even multiples appear at twice theexcitation frequency (peak 302 a), four times the excitation frequency(peak 304 a) and six times the excitation frequency (peak 306 a). As theamplitude of the excitation signal rises between 10 nanoamps and 40microamps, the amplitude of peaks 302 a, 304 a, and 306 a all increase.

FIG. 9 illustrates the effect on the even harmonic response of circuitry180 caused by harmonics modifier circuit 154. FIG. 9 illustrates a graph300 b that shows the oscillatory behavior of circuitry 180 at severalamplitudes ranging from about 30 microamps to about 100 microamps. As inFIG. 8, FIG. 9 shows a primary excitation frequency at about 6.7 MHz andsecond, fourth, and sixth order harmonics (peaks 302 b, 304 b, and 306b, respectively) appearing at even multiples of the excitationfrequency. As the amplitude of the excitation signal rises, however,between about 30 microamps to about 100 microamps, the amplitudes ofpeaks 302 b, 304 b, and 306 b do not continuously increase. Rather, theamplitude of the second order harmonics decreases rapidly above acertain transition level (e.g., about 80 microamps in FIG. 8). Thistransition level corresponds to the level at which the Zener diodesbecome conductive in the reverse biased direction and begin to affectthe oscillatory behavior of circuitry 180.

Monitoring the level at which this transition occurs may enable adetermination of a degree of coupling between primary antenna 150 andsecondary antenna 152. For example, in some embodiments, a patient mayattach external unit 120 over an area of the skin under which implantunit 110 resides. Processor 144 can proceed to cause a series ofsub-modulation control signals to be applied to primary antenna 150,which in turn cause secondary signals on secondary antenna 152. Thesesub-modulation control signals may progress over a sweep or scan ofvarious signal amplitude levels. By monitoring the resulting primarycoupled signal component on primary antenna 150 (generated throughcoupling with the secondary signal on secondary antenna 152), processor144 can determine the amplitude of primary signal (whether asub-modulation control signal or other signal) that results in asecondary signal of sufficient magnitude to activate harmonics modifiercircuit 154. That is, from a location remote from implant unit 110,processor 144 can monitor the amplitude of the second, fourth, or sixthorder harmonics and determine the amplitude of the primary signal atwhich the amplitude of any of the even harmonics drops. FIGS. 8 and 9illustrate the principles of detecting coupling through the measurementof non-linear harmonics. These Figures illustrate data based around a6.7 MHz excitation frequency. These principles, however, are not limitedto the 6.7 MHz excitation frequency illustrated, and may be used with aprimary signal of any suitable frequency.

In embodiments utilizing non-linear harmonics, the determined amplitudeof the primary signal corresponding to the transition level of the Zenerdiodes (which may be referred to as a primary signal transitionamplitude) may establish the baseline coupling range when the patientattaches external unit 120 to the skin. Thus, the initially determinedprimary signal transition amplitude may be fairly representative of anon-sleep apnea condition and may be used by processor 144 as a baselinein determining a degree of coupling between primary antenna 150 andsecondary antenna 152. Optionally, processor 144 may also be configuredto monitor the primary signal transition amplitude over a series ofscans and select the minimum value as a baseline, as the minimum valuemay correspond to a condition of maximum coupling between primaryantenna 150 and secondary antenna 152 during normal breathingconditions.

As the patient wears external unit 120, processor 144 may periodicallyscan over a range of primary signal amplitudes to determine a currentvalue of the primary signal transition amplitude. In some embodiments,the range of amplitudes that processor 144 selects for the scan may bebased on (e.g., near) the level of the baseline primary signaltransition amplitude. If a periodic scan results in determination of aprimary signal transition amplitude different from the baseline primarysignal transition amplitude, processor 144 may determine that there hasbeen a change from the baseline initial conditions. For example, in someembodiments, an increase in the primary signal transition amplitude overthe baseline value may indicate that there has been a reduction in thedegree of coupling between primary antenna 150 and secondary antenna 152(e.g., because the implant has moved or an internal state of the implanthas changed).

In addition to determining whether a change in the degree of couplinghas occurred, processor 144 may also be configured to determine aspecific degree of coupling based on an observed primary signaltransition amplitude. For example, in some embodiments, processor 144may have access to a lookup table or a memory storing data thatcorrelates various primary signal transition amplitudes with distances(or any other quantity indicative of a degree of coupling) betweenprimary antenna 150 and secondary antenna 152. In other embodiments,processor 144 may be configured to calculate a degree of coupling basedon performance characteristics of known circuit components.

By periodically determining a degree of coupling value, processor 144may be configured to determine, in situ, appropriate parameter valuesfor the modulation control signal that will ultimately result in nervemodulation. For example, by determining the degree of coupling betweenprimary antenna 150 and secondary antenna 152, processor 144 may beconfigured to select characteristics of the modulation control signal(e.g., amplitude, pulse duration, frequency, etc.) that may provide amodulation signal at electrodes 158 a, 158 b in proportion to orotherwise related to the determined degree of coupling. In someembodiments, processor 144 may access a lookup table or other datastored in a memory correlating modulation control signal parametervalues with degree of coupling. In this way, processor 144 may adjustthe applied modulation control signal in response to an observed degreeof coupling.

Additionally or alternatively, processor 144 may be configured todetermine the degree of coupling between primary antenna 150 andsecondary antenna 152 during modulation. The tongue, or other structureon or near which the implant is located, and thus implant unit 110, maymove as a result of modulation. Thus, the degree of coupling may changeduring modulation. Processor 144 may be configured to determine thedegree of coupling as it changes during modulation, in order todynamically adjust characteristics of the modulation control signalaccording to the changing degree of coupling. This adjustment may permitprocessor 144 to cause implant unit 110 to provide an appropriatemodulation signal at electrodes 158 a, 158 b throughout a modulationevent. For example, processor 144 may alter the primary signal inaccordance with the changing degree of coupling in order to maintain aconstant modulation signal, or to cause the modulation signal to bereduced in a controlled manner according to patient needs.

More particularly, the response of processor 144 may be correlated tothe determined degree of coupling. In situations where processor 144determines that the degree of coupling between primary antenna 150 andsecondary antenna has fallen only slightly below a predeterminedcoupling threshold (e.g, during snoring or during a small vibration ofthe tongue or other sleep apnea event precursor), processor 144 maydetermine that only a small response is necessary. Thus, processor 144may select modulation control signal parameters that will result in arelatively small response (e.g., a short stimulation of a nerve, smallmuscle contraction, etc.). Where, however, processor 144 determines thatthe degree of coupling has fallen substantially below the predeterminedcoupling threshold (e.g., where the tongue has moved enough to cause asleep apnea event), processor 144 may determine that a larger responseis required. As a result, processor 144 may select modulation controlsignal parameters that will result in a larger response. In someembodiments, only enough power may be transmitted to implant unit 110 tocause the desired level of response. In other words, processor 144 maybe configured to cause a metered response based on the determined degreeof coupling between primary antenna 150 and secondary antenna 152. Asthe determined degree of coupling decreases, processor 144 may causetransfer of power in increasing amounts. Such an approach may preservebattery life in the external unit 120, may protect circuitry 170 andcircuitry 180, may increase effectiveness in addressing the type ofdetected condition (e.g., sleep apnea, snoring, tongue movement, etc.),and may be more comfortable for the patient.

In some embodiments, processor 144 may employ an iterative process inorder to select modulation control signal parameters that result in adesired response level. For example, upon determining that a modulationcontrol signal should be generated, processor 144 may cause generationof an initial modulation control signal based on a set of predeterminedparameter values. If feedback from feedback circuit 148 indicates that anerve has been modulated (e.g, if an increase in a degree of coupling isobserved), then processor 144 may return to a monitoring mode by issuingsub-modulation control signals. If, on the other hand, the feedbacksuggests that the intended nerve modulation did not occur as a result ofthe intended modulation control signal or that modulation of the nerveoccurred but only partially provided the desired result (e.g, movementof the tongue only partially away from the airway), processor 144 maychange one or more parameter values associated with the modulationcontrol signal (e.g., the amplitude, pulse duration, etc.).

Where no nerve modulation occurred, processor 144 may increase one ormore parameters of the modulation control signal periodically until thefeedback indicates that nerve modulation has occurred. Where nervemodulation occurred, but did not produce the desired result, processor144 may re-evaluate the degree of coupling between primary antenna 150and secondary antenna 152 and select new parameters for the modulationcontrol signal targeted toward achieving a desired result. For example,where stimulation of a nerve causes the tongue to move only partiallyaway from the patient's airway, additional stimulation may be desired.Because the tongue has moved away from the airway, however, implant unit110 may be closer to external unit 120 and, therefore, the degree ofcoupling may have increased. As a result, to move the tongue a remainingdistance to a desired location may require transfer to implant unit 110of a smaller amount of power than what was supplied prior to the laststimulation-induced movement of the tongue. Thus, based on a newlydetermined degree of coupling, processor 144 can select new parametersfor the stimulation control signal aimed at moving the tongue theremaining distance to the desired location.

In one mode of operation, processor 144 may be configured to sweep overa range of parameter values until nerve modulation is achieved. Forexample, in circumstances where an applied sub-modulation control signalresults in feedback indicating that nerve modulation is appropriate,processor 144 may use the last applied sub-modulation control signal asa starting point for generation of the modulation control signal. Theamplitude and/or pulse duration (or other parameters) associated withthe signal applied to primary antenna 150 may be iteratively increasedby predetermined amounts and at a predetermined rate until the feedbackindicates that nerve modulation has occurred.

Processor 144 may be configured to determine or derive variousphysiologic data based on the determined degree of coupling betweenprimary antenna 150 and secondary antenna 152. For example, in someembodiments the degree of coupling may indicate a distance betweenexternal unit 120 and implant unit 110, which processor 144 may use todetermine a position of external unit 120 or a relative position of apatient's tongue. Monitoring the degree of coupling can also providesuch physiologic data as whether a patient's tongue is moving orvibrating (e.g, whether the patient is snoring), by how much the tongueis moving or vibrating, the direction of motion of the tongue, the rateof motion of the tongue, etc.

In response to any of these determined physiologic data, processor 144may regulate delivery of power to implant unit 110 based on thedetermined physiologic data. For example, processor 144 may selectparameters such as, for example, the power level and/or duration for aparticular modulation control signal or series of modulation controlsignals for addressing a specific condition relating to the determinedphysiologic data. If the physiologic data indicates that the tongue isvibrating, for example, processor 144 may determine that a sleep apneaevent is likely to occur and may issue a response by delivering power toimplant unit 110 in an amount selected to address the particularsituation. If the tongue is in a position blocking the patient's airway(or partially blocking a patient's airway), but the physiologic dataindicates that the tongue is moving away from the airway, processor 144may opt to not deliver power and wait to determine if the tongue clearson its own. Alternatively, processor 144 may deliver a small amount ofpower to implant unit 110 (e.g., especially where a determined rate ofmovement indicates that the tongue is moving slowly away from thepatient's airway) to encourage the tongue to continue moving away fromthe patient's airway or to speed its progression away from the airway.Additionally or alternatively, processor 144 may deliver power toimplant unit 110 to initiate a tongue movement, monitor the movement ofthe tongue, and deliver additional power, for example, a reduced amountof power, if necessary to encourage the tongue to continue moving awayfrom the patient's airway. The scenarios described are exemplary only.Processor 144 may be configured with software and/or logic enabling itto address a variety of different physiologic scenarios withparticularity. In each case, processor 144 may be configured to use thephysiologic data to determine an amount of power to be delivered toimplant unit 110 in order to modulate nerves associated with the tonguewith the appropriate amount of energy.

In some embodiments, processor 144 may select the parameters of aparticular modulation control signal or series of modulation controlsignals based on the severity of a physiological condition. Severity ofa detected physiological condition may be defined as a deviation fromnormal range of the condition, and may be determined by a deviation in,for example, a position of certain tissue or body parts in a subject, arate of change or direction of change in a position of certain tissue orbody parts in a subject, blood oxygen level, blood glucose level, pulserate, and breathing rate or any other parameter of normal bodilyfunction.

Processor 144 may be configured to select the parameters of a particularmodulation control signal or series of modulation control signals basedon a function (either continuous or discontinuous) of the severity ofthe detected physiological condition. In a continuous function, themeasured severity may be mapped directly to variations in the powerlevel and/or duration of the modulation control signal based on atransfer function. The transfer function may be universal,predetermined, or may be calibrated for each individual subject. In adiscontinuous function, a look-up table may be used to determined anappropriate power level and/or duration of the modulation control signalfor severities within certain ranges.

In each case, processor 144 may be configured to use the severity of thephysiologic condition to determine an amount of power to be delivered toimplant unit 110 in order to modulate nerves associated with the tonguewith the appropriate amount of energy. Because the modulation controlsignal may be received in pulses by secondary antenna 152, the lengthand frequency of the pulses of the secondary signal generated onsecondary antenna 152 may also be varied. Variations in the secondarysignal may cause variations in the power level and/or duration of themodulation signal applied to electrodes 158 a, 158 b.

A method for regulating delivery of power to implant unit 110 mayinclude detecting a severity of a physiologic condition and determining,based on the severity of the physiologic condition, a power level and/orduration of the modulation signal or series of modulation signals. Forexample, tongue movement may be indicative of a sleep disorderedbreathing event, and the amount of tongue movement may be indicative ofa severity of the sleep disordered breathing event.

In some embodiments, a predetermined movement of implant unit 110 withthe tongue muscle 130 may trigger delivery of a modulation signal. Thepredetermined movement, as used here, refers to a distance threshold, avibratory amplitude/frequency threshold, or any other suitable thresholdparameter.

The power and/or duration of the modulation signal triggered by themovement of implant unit 110 may be dependent on the amount of movementof a subject's tongue. In some embodiment, tongue movement may beindicative of sleep disordered breathing, and the amount of tonguemovement may be indicative of a severity of a sleep disordered breathingevent. The amount of tongue movement may be determined based on theabsolute movement of tongue muscle 130 relative to external unit 120.Alternatively, the amount of tongue movement may be determined by therelative displacement of implant unit 110 and external unit 120. In someembodiments, the amount of tongue movement may also refer to the speedat which the tongue is moving, direction of tongue movement, andvibration of the tongue.

As previously discussed, the degree of coupling between primary antenna150 associated with external unit 120 and secondary antenna 152associated with implant unit 110, may be monitored in order to determinean amount of tongue movement. Processor 144 may be configured to monitorthe degree of coupling and regulate delivery of power from the externalunit 120 to the implant unit 110 based on the determined degree ofcoupling and/or determined amount of tongue movement. In someembodiment, processor 144 may be configured such that a predeterminedmovement of the at least one implantable circuit with the tonguetriggers delivery of a modulation control signal. Regulation of powerdelivery in this manner, in turn, may regulate the power level and/orduration of the modulation signal applied to electrodes 158 a, 158 b.

In some embodiments, implant unit 110 may include a processor located onthe implant. A processor located on implant unit 110 may perform all orsome of the processes described with respect to the at least oneprocessor associated with an external unit. For example, a processorassociated with implant unit 110 may be configured to receive a controlsignal prompting the implant controller to turn on and cause amodulation signal to be applied to the implant electrodes for modulatinga nerve. Such a processor may also be configured to monitor varioussensors associated with the implant unit and to transmit thisinformation back to and external unit. Power for the processor unit maybe supplied by an onboard power source or received via transmissionsfrom an external unit.

In other embodiments, implant unit 110 may be self-sufficient, includingits own power source and a processor configured to operate the implantunit 110 with no external interaction. For example, with a suitablepower source, the processor of implant unit 110 could be configured tomonitor conditions in the body of a subject (via one or more sensors orother means), determining when those conditions warrant modulation of anerve, and generate a signal to the electrodes to modulate a nerve. Thepower source could be regenerative based on movement or biologicalfunction; or the power sources could be periodically rechargeable froman external location, such as, for example, through induction.

In some embodiments, the at least one processor may be associated withthe housing of external unit 120 and may be configured to communicatewith a circuit implanted in the subject. The at least one processor mayalso be configured to receive a physiological signal from the subjectvia the implanted circuit. In response to the received physiologicalsignal, the at least one processor may send a control signal, such as aclosed loop control signal, to the implanted circuit. In someembodiments, the control signal may be predetermined to activateneuromuscular tissue within the tongue. Activating neuromuscular tissuemay include, for example, causing muscular contractions and initiating anerve action potential.

The physiological signal received from the implant unit may include anysignal or signal component indicative of at least one physiologicalcharacteristic associated with the subject. In some embodiments, forexample, the physiological characteristic may indicate whether a portionof the subject's body (e.g., the tongue) has moved, a direction ofmovement, a rate of change of movement, temperature, blood pressure,etc. The physiological signal may include any form of signal suitablefor conveying information associated with at least some aspect of thesubject. In some embodiments, the physiological signal may include anelectromagnetic signal (e.g. microwave, infrared, radio-frequency (RF),etc.) having any desired waveform (e.g. sinusoidal, square wave,triangle wave, etc.). In some embodiments, the physiological signal mayinclude any suitable amplitude or duration for transferring informationabout the subject.

In some embodiments, the physiological signal may include a primarycoupled signal component on primary antenna 150. This primary coupledsignal component may be induced on primary antenna 150 through couplingbetween primary antenna 150 of external unit 120 and secondary antenna152 on implant unit 110.

In some embodiments, the physiological signal may include at least oneaspect indicative of a movement of the subject's tongue. For example,movement of the tongue may cause relative motion between primary antenna150 and secondary antenna 152, and this relative motion may result invariation of a degree of coupling between primary antenna 150 andsecondary antenna 152. By monitoring the degree of coupling betweenprimary antenna 150 and secondary antenna 152, for example, bymonitoring signals or signal components present on primary antenna 150,relative motion between primary antenna 150 and secondary antenna 152and, therefore, movement of the subject's tongue, may be detected.

As noted, in response to a received physiological signal, the at leastone processor may cause a response based on the physiological signal.For example, in some embodiments, the at least one processor may beconfigured to cause the generation of a control signal (e.g. a closedloop control signal) intended to control at least one aspect of implantunit 110. The control signal may include a modulation control signalapplied to primary antenna 150 such that a resulting secondary signal onsecondary antenna 152 will provide a modulation signal at implantelectrodes 158 a and 158 b.

In some embodiments, the processor may be configured to detect a sleepdisordered breathing event based on the physiological signal and sendthe closed loop control signal in response to the detected sleepdisordered breathing event. In some embodiments, the sleep disorderedbreathing event may be a precursor of sleep apnea, and the controlsignal may be predetermined to activate neuromuscular tissue within thetongue and may cause movement of the subject's tongue, for example, in adirection away from the posterior pharyngeal wall. The at least oneprocessor may be further configured to determine a severity of the sleepdisordered breathing event based on the physiological signal and vary apower level or duration of the control signal based on the determinedseverity of the sleep disordered breathing event. The severity of theevent may be determined, for example, based on a determination of therelative movement between primary antenna 150 and secondary antenna 152(e.g., an amplitude of movement, a rate of movement, a direction ofmovement, etc.). In some embodiments, a control signal may be sent ifthe relative movement exceeds a certain threshold.

A control signal may include any signal having suitable characteristicsfor causing a desired response in implant unit 110. For example, acontrol signal may have any suitable amplitude, duration, pulse width,duty cycle, or waveform (e.g. a sinusoidal signal, square wave, trianglewave, etc.) for causing a desired effect on implant unit 110 (e.g.,modulation of nerve tissue in the vicinity of implant unit 110, etc.). Acontrol signal may be generated and sent (e.g., to implant unit 110)within any desired response time relative to receipt of a physiologicalsignal. In some embodiments, the response time may be set at 1 second,500 milliseconds, 200 milliseconds, 100 milliseconds, 50 milliseconds,20 milliseconds, 5 milliseconds, 1 millisecond, or any other timegreater than 0 seconds and less than about 2 seconds. The control signalmay be closed loop. As used herein, the term closed loop control signalmay refer to any signal at least partially responsive to another signal,such as a control signal sent in response to a physiological signal. Orit may include any feedback response.

Based on the physiological signal, the processor may determine aquantity of energy to be sent via the closed loop control signal toimplant unit 110. The amount of energy to be sent may be determinedand/or varied based on any relevant factor including, for example, thetime of day, a relevant biological factor of the subject (bloodpressure, pulse, level of brain activity, etc.), the severity of thedetected event, other characteristics associated with the detectedevent, or on any combination of factors. As noted, in embodiments wherethe physiological signal indicates a sleep disordered breathing event,the processor may be configured to determine a severity of the sleepdisordered breathing event based on the physiological signal. In suchembodiments, the processor may also determine an amount of energy to beprovided to implant unit 110 as a response to the detected sleepdisordered breathing event and in view of the determined severity of theevent. The determined amount of energy may be transferred to implantunit 110 over any suitable time duration and at any suitable powerlevel. In some embodiments, the power level and/or the duration of thecontrol signal may be varied, and such variation may be dependent on thedetermined severity of the sleep disordered breathing event.

The power level and/or duration of the control signal may also bedetermined based on other factors. For example, the processor may vary apower level or duration associated with the control signal based on theefficiency of energy transfer between external unit 120 and implant unit110. The processor may have access to such information throughpre-programming, lookup tables, information stored in memory, etc.Additionally or alternatively, the processor may be configured todetermine the efficiency of energy transfer, e.g., by monitoring theprimary coupled signal component present on primary antenna 150, or byany other suitable method.

The processor may also vary the power level or duration of the controlsignal based on the efficacy of implant unit 110 (e.g., the implantunit's ability to produce a desired effect in response to the controlsignal). For example, the processor may determine that a certain implantunit 110 requires a certain amount of energy, a control signal of atleast a certain power level and/or signal duration, etc., in order toproduce a desired response (e.g., a modulation signal having anamplitude/magnitude of at least a desired level, etc.). Such adetermination can be based on feedback received from implant unit 110 ormay be determined based on lookup tables, information stored in memory,etc. In some embodiments, the power level or duration of the controlsignal may be determined based on a known or feedback-determinedefficacy threshold (e.g., an upper threshold at or above which a desiredresponse may be achieved) associated with implant unit 110.

In some embodiments, implant unit 110 may be structurally configured tofacilitate implantation in a location so as to increase the efficacy ofmodulation provided. For example, FIGS. 10 and 11 illustrate the anatomyof neck and tongue, and depict implantation locations suitable forneuromodulation treatment of OSA. FIG. 12 illustrates an exemplaryimplant unit 110 structurally configured for the treatment of head pain.FIGS. 13 and 14 illustrate exemplary implant units 110 structurallyconfigured for the treatment of hypertension.

FIG. 10 depicts an implantation location in the vicinity of agenioglossus muscle 1060 that may be accessed through derma on anunderside of a subject's chin. FIG. 10 depicts hypoglossal nerve (i.e.cranial nerve XII). The hypoglossal nerve 1051, through its lateralbranch 1053 and medial branch 1052, innervates the muscles of the tongueand other glossal muscles, including the genioglossus 1060, thehyoglossus, 1062, mylohyoid (not shown) and the geniohyoid 1061 muscles.The mylohyoid muscle, not pictured in FIG. 10, forms the floor of theoral cavity, and wraps around the sides of the genioglossus muscle 1060.The horizontal compartment of the genioglossus 1060 is mainly innervatedby the medial terminal fibers 1054 of the medial branch 1052, whichdiverges from the lateral branch 1053 at terminal bifurcation 1055. Thedistal portion of medial branch 1052 then variegates into the medialterminal fibers 1054. Contraction of the horizontal compartment of thegenioglossus muscle 1060 may serve to open or maintain a subject'sairway. Contraction of other glossal muscles may assist in otherfunctions, such as swallowing, articulation, and opening or closing theairway. Because the hypoglossal nerve 1051 innervates several glossalmuscles, it may be advantageous, for OSA treatment, to confinemodulation of the hypoglossal nerve 1051 to the medial branch 1052 oreven the medial terminal fibers 1054 of the hypoglossal nerve 1051. Inthis way, the genioglossus muscle, most responsible for tongue movementand airway maintenance, may be selectively targeted for contractioninducing neuromodulation. Alternatively, the horizontal compartment ofthe genioglossus muscle may be selectively targeted. The medial terminalfibers 1054 may, however, be difficult to affect with neuromodulation,as they are located within the fibers of the genioglossus muscle 1061.Embodiments of the present invention facilitate modulation the medialterminal fibers 1054, as discussed further below.

In some embodiments, implant unit 110, including at least one pair ofmodulation electrodes, e.g. electrodes 158 a, 158 b, and at least onecircuit may be configured for implantation through derma (i.e. skin) onan underside of a subject's chin. When implanted through derma on anunderside of a subject's chin, an implant unit 110 may be locatedproximate to medial terminal fibers 1054 of the medial branch 1052 of asubject's hypoglossal nerve 1051. An exemplary implant location 1070 isdepicted in FIG. 10.

In some embodiments, implant unit 110 may be configured such that theelectrodes 158 a, 158 b cause modulation of at least a portion of thesubject's hypoglossal nerve through application of an electric field toa section of the hypoglossal nerve 1051 distal of a terminal bifurcation1055 to lateral and medial branches 1053, 1052 of the hypoglossal nerve1051. In additional or alternative embodiments, implant unit 110 may belocated such that an electric field extending from the modulationelectrodes 158 a, 158 b can modulate one or more of the medial terminalfibers 1054 of the medial branch 1052 of the hypoglossal nerve 1051.Thus, the medial branch 1053 or the medial terminal fibers 1054 may bemodulated so as to cause a contraction of the genioglossus muscle 1060,which may be sufficient to either open or maintain a patient's airway.When implant unit 110 is located proximate to the medial terminal fibers1054, the electric field may be configured so as to cause substantiallyno modulation of the lateral branch of the subject's hypoglossal nerve1051. This may have the advantage of providing selective modulationtargeting of the genioglossus muscle 1060.

As noted above, it may be difficult to modulate the medial terminalfibers 1054 of the hypoglossal nerve 1051 because of their locationwithin the genioglossus muscle 1060. Implant unit 110 may be configuredfor location on a surface of the genioglossus muscle 1060. Electrodes158 a, 158 b, of implant unit 110 may be configured to generate aparallel electric field 1090, sufficient to cause modulation of themedial terminal branches 1054 even when electrodes 158 a, 158 b are notin contact with the fibers of the nerve. That is, the anodes and thecathodes of the implant may be configured such that, when energized viaa circuit associated with the implant 110 and electrodes 158 a, 158 b,the electric field 1090 extending between electrodes 158 a, 158 b may bein the form of a series of substantially parallel arcs extending throughand into the muscle tissue on which the implant is located. A pair ofparallel line electrodes or two series of circular electrodes may besuitable configurations for producing the appropriate parallel electricfield lines. Thus, when suitably implanted, the electrodes of implantunit 110 may modulate a nerve in a contactless fashion, through thegeneration of parallel electric field lines.

Furthermore, the efficacy of modulation may be increased by an electrodeconfiguration suitable for generating parallel electric field lines thatrun partially or substantially parallel to nerve fibers to be modulated.In some embodiments, the current induced by parallel electric fieldlines may have a greater modulation effect on a nerve fiber if theelectric field lines 1090 and the nerve fibers to be modulated arepartially or substantially parallel. The inset illustration of FIG. 10depicts electrodes 158 a and 158 b generating electric field lines 1090(shown as dashed lines) substantially parallel to medial terminal fibers1054.

In order to facilitate the modulation of the medial terminal fibers1054, implant unit 110 may be designed or configured to ensure theappropriate location of electrodes when implanted. An exemplaryimplantation is depicted in FIG. 11.

For example, a flexible carrier 161 of the implant may be configuredsuch that at least a portion of a flexible carrier 161 of the implant islocated at a position between the genioglossus muscle 1060 and thegeniohyoid muscle 1061. Flexible carrier 161 may be further configuredto permit at least one pair of electrodes arranged on flexible carrier161 to lie between the genioglossus muscle 1060 and the mylohyoidmuscle. Either or both of the extensions 162 a and 162 b of elongate arm161 may be configured adapt to a contour of the genioglossus muscle.Either or both of the extensions 162 a 162 b of elongate arm 161 may beconfigured adapt to a contour of the genioglossus muscle. Either or bothof the extensions 162 a and 162 b of elongate arm 161 may be configuredto extend away from the underside of the subject's chin along a contourof the genioglossus muscle 1060. Either or both of extension arms 162 a,162 b may be configured to wrap around the genioglossus muscle when anantenna 152 is located between the genioglossus 1060 and geniohyoidmuscle 1061. In such a configuration, antenna 152 may be located in aplane substantially parallel with a plane defined by the underside of asubject's chin, as shown in FIG. 11.

Flexible carrier 161 may be configured such that the at least one pairof spaced-apart electrodes can be located in a space between thesubject's genioglossus muscle and an adjacent muscle. Flexible carrier161 may be configured such that at least one pair of modulationelectrodes 158 a, 158 b is configured for implantation adjacent to ahorizontal compartment 1065 of the genioglossus muscle 1060. Thehorizontal compartment 1065 of the genioglossus 1060 is depicted in FIG.11 and is the portion of the muscle in which the muscle fibers run in asubstantially horizontal, rather than vertical, oblique, or transversedirection. At this location, the hypoglossal nerve fibers run betweenand in parallel to the genioglossus muscle fibers. In such a location,implant unit 110 may be configured such that the modulation electrodesgenerate an electric field substantially parallel to the direction ofthe muscle fibers, and thus, the medial terminal fibers 1054 of thehypoglossal nerve in the horizontal compartment.

FIG. 12 depicts an exemplary implant location for the treatment of headpain. As illustrated in FIG. 12, implant unit 510 includes an elongatedcarrier 561, secondary antenna 552, and modulation electrodes 558 a, 558b. Implant unit 510 may also include any elements, such as circuitry,electrical components, materials, and any other features describedpreviously with respect to implant unit 110. Implant 510 may be sizedand configured such that it may be implanted with an end havingsecondary antenna 552 located beneath the skin in a substantiallyhairless region 507 of a subject. Elongated flexible carrier 561 mayextend from this location, across a hairline 502 of the subject, to alocation beneath the skin in a substantially haired region 506 of thesubject in a vicinity of an occipital or other nerve that may bemodulated to control or reduce head pain, such as a greater occipitalnerve 501 or a lesser occipital nerve 503. As used herein, the term“substantially haired region” includes areas of a subject's head locatedon a side of the hairline where the scalp hair is located on a typicalsubject. Thus, a bald person may still have a “substantially hairedregion” on the side of the hairline on which hair typically grows. Asused herein, the term “substantially hairless region” includes areas ofa subject's head located on a side of the hairline where the scalp hairis not located on a typical subject. A “substantially hairless region,”as used herein, is not required to be completely hairless, as almost allskin surfaces have some hair growth. As illustrated in FIG. 12, asubstantially haired region 506 is separated from a substantiallyhairless region 507 by a hairline 502.

As described above, implant 510 may extend across the hairline 502 to alocation in the vicinity of an occipital nerve. In FIG. 12, implant 510extends across the hairline 502 to a location in the vicinity of greateroccipital nerve 501. Furthermore, implant 510 may be configured forimplantation such that electrodes 558 a and 558 b are spaced from eachother along a longitudinal direction of an occipital nerve, such as thegreater occipital nerve 501 shown in FIG. 12. Such a configurationpermits electrodes 558 a and 558 b to facilitate an electrical fieldthat extends in the longitudinal direction of the occipital nerve. Inturn, the facilitated electrical field may be utilized to modulategreater occipital nerve 501, for example to block pain signals, aspreviously described.

The size and configuration of implant 510 illustrated in FIG. 12 maypermit secondary antenna 552 to be located beneath the skin in alocation where an external unit 520 (not illustrated), may be easilyaffixed to the skin, due to the lack of hair. External unit 520 mayinclude any elements, such as circuitry, processors, batteries,antennas, electrical components, materials, and any other featuresdescribed previously with respect to external unit 120. External unit520 may be configured to communicate with implant 510 via secondaryantenna 552 to deliver power and control signals, as described abovewith respect to external unit 120. Elongated carrier 561 may beflexible, and may permit modulation electrodes 558 a and 558 b to belocated beneath the skin in a location suitable for modulating anoccipital or other nerve for controlling head pain.

FIG. 13 depicts an exemplary implant location for the treatment ofhypertension. As illustrated in FIG. 13, implant unit 610 may beconfigured for location or implantation inside a blood vessel. Such aconfiguration may include, for example, a flexible tubular carrier.Implant unit 610 may also include any elements, such as circuitry,electrical components, materials, and any other features describedpreviously with respect to implant unit 110. Implant unit 610 mayinclude modulation electrodes 658 a, 658 b configured to facilitate anelectric field including field lines extending in the longitudinaldirection of the blood vessel. For example, as illustrated in FIG. 13,implant unit 610 may be implanted in a carotid artery 611. Implant unit610 may be located within carotid artery 611 in a location in thevicinity of carotid baroreceptors 615, at a location near the branchingof the internal carotid artery 613 and the external carotid artery 612.As described previously, carotid baroreceptors 615 aid in the regulationof the blood pressure of a subject. Thus, implant unit 610, locatedwithin carotid artery 611 in the vicinity of carotid baroreceptors 615may facilitate an electric field configured to modulate carotidbaroreceptors 615, and, thus, affect the blood pressure of a subject.Affecting the blood pressure of a subject may include reducing,increasing, controlling, regulating, and influencing the blood pressureof a subject. The illustrated location is exemplary only, and implantunit 610 may be configured in alternate ways. For example, implant unit610 may be configured for implantation in jugular vein 614 of thesubject, in a location from which modulation of carotid baroreceptors615 may be accomplished. Furthermore, implant unit 610 may be configuredfor implantation in a blood vessel, such as carotid artery 611 orjugular vein 614, in a location suitable for modulation ofglossopharyngeal nerve 615. As described above, glossopharyngeal nerve615 innervates carotid baroreceptors 615. Thus, glossopharyngeal nerve615 may be directly modulated to affect blood pressure of a subject.Glossopharyngeal nerve 615 may also be modulated by an implant unit 610located in a sub-cutaneously, in a non-intravascular location.

FIG. 14 depicts another exemplary implant location for the treatment ofhypertension. As illustrated in FIG. 14, implant unit 710 may beconfigured for location or implantation inside a blood vessel. Such aconfiguration may include, for example, a flexible tubular carrier.Implant unit 710 may also include any elements, such as circuitry,electrical components, materials, and any other features describedpreviously with respect to implant unit 110. Implant unit 710 mayinclude modulation electrodes 758 a, 758 b configured to facilitate anelectric field including field lines extending in the longitudinaldirection of the blood vessel. For example, as illustrated in FIG. 13,implant unit 710 may be implanted in a renal artery 711. Implant unit710 may be located within renal artery 711 in a location in the vicinityof renal nerves 715 surrounding renal artery 711 prior to its entry intokidney 712. As described previously, renal nerves 715 aids in theregulation of the blood pressure in humans. Thus, implant unit 710,located within renal artery 711 in the vicinity of renal nerves 715 mayfacilitate an electric field configured to modulate renal nerves 715,and, thus, affect the blood pressure of a subject. The illustratedlocation is exemplary only, and implant unit 710 may be configured inalternate ways suitable for the modulation of renal nerves 715.

Other embodiments of the present disclosure will be apparent to thoseskilled in the art from consideration of the specification and practiceof the present disclosure.

While this disclosure provides examples of the neuromodulation devicesemployed for the treatment of certain conditions, usage of the disclosedneuromodulation devices is not limited to the disclosed examples. Thedisclosure of uses of embodiments of the invention for neuromodulationare to be considered exemplary only. In its broadest sense, theinvention may be used in connection with the treatment of anyphysiological condition through neuromodulation. Alternative embodimentswill become apparent to those skilled in the art to which the presentinvention pertains without departing from its spirit and scope.Accordingly, the scope of the present invention is defined by theappended claims rather than the foregoing description.

What is claimed:
 1. A sleep disordered breathing therapy device,comprising: at least one implantable circuit; and at least one pair ofimplantable electrodes in electrical communication with the circuit, theat least one implantable circuit and at least one pair of implantableelectrodes being configured for implantation in a vicinity of agenioglossus muscle of a subject, the at least one pair of implantableelectrodes being configured to modulate a hypoglossal nerve; wherein theat least one implantable circuit is configured to deliver a power signalto the at least one pair of implantable electrodes, wherein the powersignal has at least one of a power level and a duration determined basedon a severity of a detected physiological condition.
 2. The device ofclaim 1, wherein the implantable circuit is further configured todeliver the power signal in response to a received signal indicative ofthe severity of the physiological condition.
 3. The device of claim 1,wherein the physiological condition includes tongue movement, andwherein at least one of the power level or duration of the power signaldelivered by the circuit to the electrodes is based on an amount oftongue movement.
 4. The device of claim 1, wherein an amount of tonguemovement includes at least one of speed of the tongue, vibration of thetongue, and displacement of the tongue.
 5. The device of claim 2,wherein the at least one implantable circuit is configured forimplantation on a tongue muscle of a subject, and wherein the at leastone implantable circuit is configured such that a predetermined movementof the at least one implantable circuit with the tongue triggersdelivery of the received signal.
 6. The device of claim 3, wherein thetongue movement is indicative of a sleep disordered breathing and theamount of tongue movement is indicative of a severity of the sleepdisordered breathing event.
 7. The device of claim 2, further comprisingan antenna, wherein the antenna is adapted to receive a transmittedalternating current signal; and a signal modifier configured to convertthe alternating current signal into a direct current signal for deliveryto the at least one pair of implantable electrodes.
 8. A method ofregulating energy delivery to an implanted circuit for treating a sleepdisordered breathing condition, the method comprising: detecting aseverity of a physiological condition in a body of a subject;determining, based on the severity of the physiological condition, atleast one of a power level or a duration of a power signal to bedelivered by the implanted circuit to at least one pair of electrodesimplanted proximal to a hypoglossal nerve of the subject and inelectrical communication with the implanted circuit; delivering thepower signal to the at least one pair of electrodes; modulating thehypoglossal nerve of the subject via the power signal.
 9. The method ofclaim 8, further comprising delivering the power signal in response toat least one received signal indicative of the severity of thephysiological condition.
 10. The method of claim 8, wherein the detectedphysiological condition includes tongue movement, and wherein at leastone of the power level or duration of the signal to be delivered to theelectrodes is based on an amount of tongue movement.
 11. The method ofclaim 10, wherein an amount of tongue movement includes at least one ofspeed of the tongue, vibration of the tongue, and displacement of thetongue.
 12. The method of claim 8, wherein the implanted circuit isimplanted on a tongue muscle of the subject, and wherein delivery of thepower signal is triggered by a predetermined motion of the implantedcircuit with the tongue.
 13. The method of claim 10, wherein the tonguemovement is indicative of a sleep disordered breathing event, and theamount of tongue movement is indicative of a severity of the sleepdisordered breathing event.
 14. The method of claim 7, furthercomprising transmitting an alternating current signal to the implantedcircuit; and converting the alternating current signal into a directcurrent signal, wherein the signal delivered to the electrodes is thedirect current signal.
 15. A device, comprising: at least oneimplantable circuit; and at least one pair of implantable electrodes inelectrical communication with the circuit, the at least one pair ofimplantable electrodes being configured to modulate at least one nerve;wherein the at least one implantable circuit is configured to deliver apower signal to the at least one pair of implantable electrodes, whereinthe power signal has at least one of a power level and a durationdetermined based on a severity of a detected physiological condition.16. A hypertension treatment device for affecting blood pressure,comprising: a flexible carrier configured for implantation in a bloodvessel of a subject; at least one implantable circuit; and at least onepair of implantable electrodes in electrical communication with thecircuit and located on the flexible carrier, the at least one pair ofimplantable electrodes being configured to modulate at least one of arenal nerve, a baroreceptor, and a glossopharyngeal nerve; wherein theat least one implantable circuit is configured to deliver a power signalto the at least one pair of implantable electrodes, wherein the powersignal has at least one of a power level and a duration determined basedon a severity of a detected physiological condition.
 17. Thehypertension treatment device of claim 16, wherein the physiologicalcondition includes blood pressure, and wherein at least one of the powerlevel or duration of the power signal delivered by the circuit to theelectrodes is based on a level of blood pressure.